نتایج جستجو برای: phalanges and clavicles

تعداد نتایج: 16827265  

Journal: :Journal of medical genetics 1989
R C Hennekam C Vermeulen-Meiners

A boy with intrauterine growth retardation, microcephaly, dysostosis of the skull, hypoplastic facial bones, labiogingival retraction, agenesis of the clavicles, distal aphalangia, and severely hypoplastic thumbs and halluces is described. The features are consistent with the Yunis-Varon syndrome. Review of published reports shows this to be a generalised disorder with variable manifestations i...

2016
H. K. Lewis

This volume is founded on a short course of post-graduate lectures, delivered in Glasgow in 1890. It contains a short outline of the literature of the subject, and then gives illustrative cases of the principal groups of mediastinal growths. In considering the question of diagnosis, the author refers especially to the following useful points : 1. The development of fulness and nodular or glandu...

Jamali, M,

Different opinions exit in histological typing of bone cysts. Epidermoid cysts are very rare as the small numbers of published cases indicate. They arises following preceding trauma exclusively in distal phalanges and skull. The roentgenogram shows a round osteolytic resion with no trabecular pattern. We observed 2 cases of epidermoid cyst of finger in Imam Khomeini hospital central path depart...

2016
Bau-Lin Huang Anna Trofka Aki Furusawa Jacqueline L Norrie Adam H Rabinowitz Steven A Vokes M Mark Taketo Jozsef Zakany Susan Mackem

The number of phalanges and joints are key features of digit 'identity' and are central to limb functionality and evolutionary adaptation. Prior chick work indicated that digit phalanges and their associated joints arise in a different manner than the more sparsely jointed long bones, and their identity is regulated by differential signalling from adjacent interdigits. Currently, there is no ge...

2014
Minal ShaStri Mital PariKh Dwijal Patel Ketan ChuDaSMa ruShaD Patell

SPG (Symmetrical peripheral gangrene) is defined as symmetrical distal ischemic damage at two or more sites in the absence of large vessels obstruction. It has been ascribed to a number of infectious and non infectious conditions including connective tissue, cardiovascular, neoplastic and iatrogenic causes. We report a unique case of SPG in a 35-year-old Indian female who developed spontaneous ...

Journal: :British journal of sports medicine 1994
S R Bollen V Wright

Radiographs of the hands of 36 rock climbers were compared with radiographs of the hands of controls matched for age and sex. Subchondral cysts were present in the hands of 17 climbers and only two controls. Osteophytes or bony spurs were present in 14 climbers but not in any of the controls, and the only two cases of frank osteoarthrosis were in the hands of climbers. Cortical thickness of the...

Journal: :Journal of medical genetics 1998
E F Percin S Percin H Egilmez I Sezgin F Ozbas A N Akarsu

Syndactyly type I is an autosomal dominant condition with complete or partial webbing between the third and fourth fingers or the second and third toes or both. We report here a previously undescribed phenotype of severe mesoaxial syndactyly and synostosis in patients born to affected parents. The characteristic features of these severe cases are (1) complete syndactyly and synostosis of the th...

2016
J. Maitland

This patient was a Hindoo, 22 years of age. Description of the deformity.?The bones of the second and third toes of the left foot are very much enlarged. Each toe measures three inches in length and two and a half inches in circumference. The terminal phalanges are slightly curved towards one another, giving the part a claw-like appearance. The metatarsal bones are enlarged proportionately to t...

Journal: :Collegium antropologicum 2007
Roberto Buffa Elisabetta Marini Stefano Cabras Giuliana Scalas Giovanni Floris

This study is an analysis of the patterns of variation of the human hand, particularly the metric characters of palm, fingers and distal phalanges. Anthropometric measurements were performed on 146 Sardinian men and women, aged 21 to 31 years. The data were analyzed by inferential statistics (paired Student's t test, analysis of variance), and Principal Components Analysis. The results indicate...

Journal: :Annales Academiae Medicae Stetinensis 2008
Aleksandra Gawlikowska-Sroka

Polydactyly is a common hereditary disorder in which extra or vestigial digits are present on the one or both sides of the extremities. It is ten times more frequent in Blacks than in Whites. Polydactyly occurs both in a sporadic form and in a hereditary form. In polydactyly type A, the extra digits contains phalanges, in polydactyly type B, there is no skeletal structure. The extra digit is ma...

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